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pro vyhledávání: '"transmembrane protein 230"'
Autor:
Franco Cotelli, Rolland Reinbold, Lorenzo Sangiorgio, Gianluca Deflorian, Paride Pelucchi, Alberto Albertini, Antonio Giordano, Ileana Zucchi, James Kehler, Alessandra Mezzelani, Gianfranco Bellipanni, Silvia Carra, Mira Palizban, Solei Cermenati, Martin Götte, Valentina Martino, Monica Beltrame
Publikováno v:
Journal of cellular physiology
(2017): 1455–1467. doi:10.1002/jcp.26032
info:cnr-pdr/source/autori:Carra S.; Sangiorgio L.; Pelucchi P.; Cermenati S.; Mezzelani A.; Martino V.; Palizban M.; Albertini A.; Götte M.; Kehler J.; Deflorian G.; Beltrame M.; Giordano A.; Reinbold R.; Cotelli F.; Bellipanni G.; Zucchi I./titolo:Zebrafish Tmem230a cooperates with the Delta%2FNotch signaling pathway to modulate endothelial cell number in angiogenic vessels/doi:10.1002%2Fjcp.26032/rivista:Journal of cellular physiology (Print)/anno:2017/pagina_da:1455/pagina_a:1467/intervallo_pagine:1455–1467/volume
(2017): 1455–1467. doi:10.1002/jcp.26032
info:cnr-pdr/source/autori:Carra S.; Sangiorgio L.; Pelucchi P.; Cermenati S.; Mezzelani A.; Martino V.; Palizban M.; Albertini A.; Götte M.; Kehler J.; Deflorian G.; Beltrame M.; Giordano A.; Reinbold R.; Cotelli F.; Bellipanni G.; Zucchi I./titolo:Zebrafish Tmem230a cooperates with the Delta%2FNotch signaling pathway to modulate endothelial cell number in angiogenic vessels/doi:10.1002%2Fjcp.26032/rivista:Journal of cellular physiology (Print)/anno:2017/pagina_da:1455/pagina_a:1467/intervallo_pagine:1455–1467/volume
During embryonic development, new arteries and veins form from preexisting vessels in response to specific angiogenic signals. Angiogenic signaling is complex since not all endothelial cells exposed to angiogenic signals respond equally. Some cells w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6e05326b9ee05fa6ab1b04c3789c589
https://doi.org/10.1002/jcp.26032
https://doi.org/10.1002/jcp.26032
Publikováno v:
Journal of Clinical Movement Disorders
Mutations in six genes are known to cause Parkinson’s disease (PD) (autosomal dominant: alpha-synuclein, LRRK2, VPS35 and autosomal recessive: Parkin, PINK1 and DJ1) and number of other genes are implicated. In a recent article Deng and colleagues
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89900dc27949ad019af0d6818cab210a
https://pubmed.ncbi.nlm.nih.gov/27872751
https://pubmed.ncbi.nlm.nih.gov/27872751
Akademický článek
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Autor:
Olszewska DA; Department of Neurology, Dublin Neurological Institute at the Mater Misericordiae University Hospital, Dublin, Ireland., Fearon C; Department of Neurology, Dublin Neurological Institute at the Mater Misericordiae University Hospital, Dublin, Ireland ; Department of Neurology, Cork University Hospital, Cork, Ireland., Lynch T; Department of Neurology, Dublin Neurological Institute at the Mater Misericordiae University Hospital, Dublin, Ireland.
Publikováno v:
Journal of clinical movement disorders [J Clin Mov Disord] 2016 Nov 15; Vol. 3, pp. 17. Date of Electronic Publication: 2016 Nov 15 (Print Publication: 2016).